Pangenome read alignment and variant calling

Pan-genome references, also known as graph reference genomes, can represent multiple strains in a single reference structure. To utilize them fully, we need tools to employ them as we currently use single references. In this project, we aimed to tackle two important sequence analysis tasks and transform them to graph-based references: read-alignment and variant calling.

Share this post

Share on facebook
Share on twitter
Share on linkedin
Share on print
Share on email